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57409-51-5

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57409-51-5 Usage

Chemical Properties

Yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 57409-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,0 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57409-51:
(7*5)+(6*7)+(5*4)+(4*0)+(3*9)+(2*5)+(1*1)=135
135 % 10 = 5
So 57409-51-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O4S/c1-13-9(12)7(11)5-6(10)8-3-2-4-14-8/h2-4H,5H2,1H3

57409-51-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H61396)  Methyl 2,4-dioxo-4-(2-thienyl)butyrate, 97%   

  • 57409-51-5

  • 250mg

  • 200.0CNY

  • Detail
  • Alfa Aesar

  • (H61396)  Methyl 2,4-dioxo-4-(2-thienyl)butyrate, 97%   

  • 57409-51-5

  • 1g

  • 872.0CNY

  • Detail

57409-51-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2,4-dioxo-4-(thiophen-2-yl)butanoate

1.2 Other means of identification

Product number -
Other names methyl 2,4-dioxo-4-thiophen-2-ylbutanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57409-51-5 SDS

57409-51-5Relevant articles and documents

Design, synthesis, biological evaluation and in silico studies of pyrazole‐based nh2‐acyl oseltamivir analogues as potent neuraminidase inhibitors

Ye, Jiqing,Lin, Lin,Xu, Jinyi,Chan, Paul Kay-Sheung,Yang, Xiao,Ma, Cong

, (2021/05/05)

Oseltamivir represents one of the most successful neuraminidase (NA) inhibitors in the current anti‐influenza therapy. The 150‐cavity of NA was identified as an additional binding pocket, and novel NA inhibitors have been designed to occupy the 150‐cavity

CYCLIC SULFAMIDE COMPOUNDS FOR TREATMENT OF HBV

-

Page/Page column 48; 52-53vi-, (2020/03/29)

The present disclosure provides, in part, cyclic sulfamide compounds, and pharmaceutical compositions thereof, useful for disruption of HBV core protein assembly, and methods of treating Hepatitis B (HBV) infection.

CYCLIC SULFAMIDE COMPOUNDS AND METHODS OF USING SAME

-

Page/Page column 61; 69, (2018/09/21)

The present disclosure provides, in part, cyclic sulfamide compounds, and pharmaceutical compositions thereof, useful as modulators of Hepatitis B (HBV) core protein, and methods of treating Hepatitis B (HBV) infection.

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